U.S. patent application number 10/156309 was filed with the patent office on 2003-01-30 for cosmetic formulations of quaternary ammonium compounds incorporating polyhydric alcohols.
This patent application is currently assigned to Clariant GmbH. Invention is credited to Gatter, Erich, Klein, Sonja, Milbradt, Robert, Oberhauser, Adelgunde, Scherl, Franz Xaver.
Application Number | 20030021759 10/156309 |
Document ID | / |
Family ID | 7686595 |
Filed Date | 2003-01-30 |
United States Patent
Application |
20030021759 |
Kind Code |
A1 |
Milbradt, Robert ; et
al. |
January 30, 2003 |
Cosmetic formulations of quaternary ammonium compounds
incorporating polyhydric alcohols
Abstract
Cosmetic, dermatological and pharmaceutical compositions
containing quaternary ammonium compounds, particularly for
hair-treatment, require low setting points, good solubility and
dispersibility in aqueous media and a low flash point. It has now
been found that such compositions can be formulated with quaternary
ammonium compounds and polyhydric alcohols. The invention provides
compositions comprising a) at least one quaternary ammonium
compound, b) at least one branched alcohol having 8 to 36 carbon
atoms or a mixture of at least one branched alcohol and at least
one unbranched alcohol having 8 to 36 carbon atoms, and c) at least
one polyhydric alcohol having 2 to 6 carbon atoms. The resulting
compositions have a low setting point or melting point, good
solubility and dispersibility in aqueous media and a low flash
point.
Inventors: |
Milbradt, Robert;
(Wlesbaden, DE) ; Klein, Sonja; (Hattershelm,
DE) ; Scherl, Franz Xaver; (Burgkirchen, DE) ;
Gatter, Erich; (Kastl, DE) ; Oberhauser,
Adelgunde; (Neuotting, DE) |
Correspondence
Address: |
CLARIANT CORPORATION
INTELLECTUAL PROPERTY DEPARTMENT
4000 MONROE ROAD
CHARLOTTE
NC
28205
US
|
Assignee: |
Clariant GmbH
|
Family ID: |
7686595 |
Appl. No.: |
10/156309 |
Filed: |
May 28, 2002 |
Current U.S.
Class: |
424/70.28 ;
514/642 |
Current CPC
Class: |
C11D 3/202 20130101;
A61Q 19/00 20130101; C11D 1/62 20130101; A61K 8/34 20130101; A61Q
5/10 20130101; A61Q 5/065 20130101; A61Q 5/12 20130101; Y10S 424/01
20130101; A61Q 5/02 20130101; A61Q 5/06 20130101; A61K 8/342
20130101; A61Q 5/08 20130101; A61K 8/345 20130101; A61Q 5/00
20130101; C11D 3/2041 20130101; A61Q 5/04 20130101; A61Q 19/10
20130101; A61K 8/046 20130101; C11D 3/2017 20130101; Y10S 514/937
20130101; A61K 8/416 20130101 |
Class at
Publication: |
424/70.28 ;
514/642 |
International
Class: |
A61K 007/075; A61K
007/08; A61K 031/14 |
Foreign Application Data
Date |
Code |
Application Number |
May 29, 2001 |
DE |
101 26 253.1 |
Claims
1. A composition comprising a) at least one quaternary ammonium
compound according to formula (1) 2where R.sub.1 is an unbranched
or branched alkyl or alkenyl group having 12 to 36 carbon atoms, a
group R.sub.5CONH(CH.sub.2).sub.n-- or a group
R.sub.5COO(CH.sub.2).sub.n--, where R.sub.5 is an alkyl or alkenyl
group having 12 to 36 carbon atoms and n is a number from 1 to 8,
and R.sub.2, R.sub.3 and R.sub.4, independently of one another, may
be identical or different and are a --CH.sub.3, CH.sub.3CH.sub.2--,
CH.sub.3CH.sub.2CH.sub.2--, CH.sub.3CH.sub.2CH.sub.2CH.sub.2--,
--CH.sub.2CH.sub.2OH or --CH.sub.2CH(OH)CH.sub.2OH group and
X.sup.- is an anion, and b) at least one branched alcohol b1)
having 8 to 36 carbon atoms or a mixture of at least one branched
alcohol b1) and at least one unbranched alcohol b2) having 8 to 36
carbon atoms, and c) at least one polyhydric alcohol having 2 to 6
carbon atoms.
2. The composition as claimed in claim 1, which comprises, as
component b), a mixture of at least one branched alcohol b1) and at
least one unbranched alcohol b2).
3. The composition as claimed in claim 1, wherein the content of
quaternary ammonium compounds a), based on the finished
composition, is 30 to 90% by weight.
4. The composition as claimed in claim 1, wherein the quaternary
ammonium compounds a) are
(C.sub.12-C.sub.36)-alkyltrimethylammonium compounds.
5. The composition as claimed in claim 1, wherein the anion X.sup.-
in formula (1) is selected from the group consisting of chloride,
iodide, bromide, methosulfate, hydrogensulfate, lactate, citrate,
and mixtures thereof.
6. The composition as claimed in claim 1, wherein the quaternary
ammonium compound a) is behenyltrimethylammonium chloride.
7. The composition as claimed in claim 1, wherein the content of
alcohols b), based on the finished composition, is 10 to 60% by
weight.
8. The composition as claimed in claim 1, wherein the weight ratio
of branched alcohols b1) to unbranched alcohols b2) is 90:10 to
10:90.
9. The composition as claimed in claim 1, wherein the branched
alcohols b1) and the unbranched alcohols b2) each have 10 to 24
carbon atoms.
10. The composition as claimed in at least one of claims 1, wherein
the branched alcohols b1) are Guerbet alcohols selected from the
group consisting of 2-methyl-1-decanol, 2-ethyl-1-nonanol,
2-propyl-1-octanol, 2-butyloctanol, 2-butyldecanol, 2-hexyloctanol,
2-hexyldecanol, 2-octyldecanol, 2-hexyldodecanol, 2-octyldodecanol,
2-decyltetradecanol, 2-butyl-1-heptanol, 2-dodecylhexadecanol,
tetradecyloctadecanol, 2-tetradecyleicosanol,
2-hexadecyloctadecanol, 2-hexadecyleicosanol, 2-methyltridecanol,
2-ethyldodecanol, 2-propylundecanol, 2-pentylnonanol,
2-heptylheptanol, 2-methyltetradecanol, 2-ethyltridecanol,
2-propyldodecanol, 2-butylundecanol, 2-pentyldecanol,
2-hexylnonanol, 2-heptyloctanol, isotridecyl alcohol, and mixtures
thereof.
11. The composition as claimed in claim 1, wherein the unbranched
alcohols b2) are fatty alcohols selected from the group consisting
of lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl
alcohol, eicosanyl alcohol, behenyl alcohol, nonanol, undecanol,
tridecanol, pentadecanol ,heptadecanol, and mixtures thereof.
12. The composition as claimed in claim 1, wherein the content of
polyhydric alcohols c), based on the finished composition, is 0.5
to 20% by weight.
13. The composition as claimed in claim 1, wherein the polyhydric
alcohols c) are selected from the group consisting of glycols,
butanediols, glycerol, thioglycerol, sorbitol, xylitol, mannitol,
and mixtures thereof.
14. The composition as claimed in claim 1, which comprises
unbranched or branched monoalcohols having 1 to 4 carbon atoms.
15. The composition as claimed in claim 14, which comprises, based
on the finished composition, less than 5% by weight, of the
unbranched or branched monoalcohols having 1 to 4 carbon atoms.
16. The composition as claimed in claim 1, which has a setting
point below 100.degree. C.
17. The composition as claimed in claim 1, which has a flash point
above 80.degree. C.
18. The composition as claimed in claim 1, which is in the form of
pellets, flakes, extrudates, pastes, compacts, powders, emulsions
or dispersions.
19. A process for the preparation of compositions as claimed in
claim 1, which comprises preparing a mixture comprising i) at least
one quaternary ammoniun compound a), ii) at least one branched
alcohol b1) having 8 to 36 carbon atoms or a mixture of at least
one branched alcohol b1) and at least one unbranched alcohol b2)
having 8 to 36 carbon atoms, and iii) at least one polyhydric
alcohol c).
20. A process for the preparation of a composition as claimed in
claim 1, which comprises alkylating i) at least one tertiary amine
NR.sub.1R.sub.2R.sub.3, where R.sub.1 is an unbranched or branched
alkyl or alkenyl group having 12 to 36 carbon atoms, a group
R.sub.5CONH(CH.sub.2).sub.n-- or a group
R.sub.5COO(CH.sub.2).sub.n--, where R.sub.5 is an alkyl or alkenyl
group having 12 to 36 carbon atoms and n is a number from 1 to 8,
and R.sub.2 and R.sub.3, independently of one another, may be
identical or different and are CH.sub.3--, CH.sub.3CH.sub.2--,
CH.sub.3CH.sub.2CH.sub.2--, CH.sub.3CH.sub.2CH.sub.2C- H.sub.2-- or
--CH.sub.2CH.sub.2(OH), by ii) at least one alkylating agent chosen
from a) R.sub.4X, where R.sub.4 is CH.sub.3--, CH.sub.3CH.sub.2--,
CH.sub.3CH.sub.2CH.sub.2--, CH.sub.3CH.sub.2CH.sub.2CH.sub.2-- or
--CH.sub.2CH(OH)CH.sub.2(OH), and X is Cl, I, Br, OSO.sub.3H or
methosulfate, and/or b) ethylene oxide and an acid HX, where X is
Cl, I, Br, OSO.sub.3H, citrate or lactate, in the presence of iii)
at least one branched alcohol b1) having 8 to 36 carbon atoms or a
mixture of at least one branched alcohol b1) and one unbranched
alcohol b2) having 8 to 36 carbon atoms and iv) at least one
polyhydric alcohol c).
21. The composition as claimed in claim 1, wherein the content of
quaternary ammonium compounds a), based on the finished
composition, is 50 to 90% by weight.
22. The composition as claimed in claim 1, wherein the quaternary
ammonium compounds a) are
(C.sub.14-C.sub.30)-alkyltrimethylammonium compounds.
23. The composition as claimed in claim 1, wherein the quaternary
ammonium compounds a) are
(C.sub.16-C.sub.24)-alkyltrimethylammonium compounds.
24. The composition as claimed in claim 1, wherein the anion
X.sup.- in formula (1) is chloride and/or methosulfate.
25. The composition as claimed in claim 1, wherein the content of
alcohols b), based on the finished composition, is 10 to 50% by
weight.
26. The composition as claimed in claim 1, wherein the content of
alcohols b), based on the finished composition, is 20 to 40% by
weight.
27. The composition as claimed in claim 1, wherein the weight ratio
of branched alcohols b1) to unbranched alcohols b2) is 70:30 to
30:70.
28. The composition as claimed in claim 1, wherein the weight ratio
of branched alcohols b1) to unbranched alcohols b2) is 60:40 to
40:60.
29. The composition as claimed in claim 1, wherein the branched
alcohols b1) and the unbranched alcohols b2) each have 12 to 18
carbon atoms.
30. The composition as claimed in claim 1, wherein the branched
alcohols b1) and the unbranched alcohols b2) each have 14 to 16,
carbon atoms.
31. The composition as claimed in claim 1, wherein the content of
polyhydric alcohols c), based on the finished composition, is 0.5
to 10% by weight.
32. The composition as claimed in claim 1, wherein the polyhydric
alcohols c) are selected from the group consisting of ethylene
glycol, propylene glycol, 1,3-butanediol, and mixtures thereof.
33. The composition as claimed in claim 14, wherein the unbranched
or branched monoalcohols having 1 to 4 carbon atoms comprises
isopropanol.
34. The composition as claimed in claim 14, which comprises, based
on the finished composition, less than 1% by weight, of the
unbranched or branched monoalcohols having 1 to 4 carbon atoms.
35. The composition as claimed in claims 1, which has a setting
point below 95.degree. C.
36. The composition as claimed in claims 1, which has a setting
point below 90.degree. C.
37. The composition as claimed in claims 1, which has a setting
point below 85.degree. C.
38. The composition as claimed in at least one of claims 1 to 16,
which has a flash point above 100.degree. C.
39. The process of claim 19 further comprising adding a branched or
unbranched monoalcohol having 1 to 4 carbon atoms.
40. The process of claim 20 further comprising conducting said
alkylating in the presence of a branched or unbranched monoalcohol
having 1 to 4 carbon atoms.
41. A cosmetic preparation comprising the composition of claim
1.
42. A dermatological preparation comprising the composition of
claim 1.
43. A pharmaceutical preparation comprising the composition of
claim 1.
44. A hair-treatment composition comprising the composition of
claim 1.
45. The hair-treatment composition as defined in claim 46 in the
form of shampoos, rinse-off hair conditioners, cream rinses, clear
rinses, hair cures, hair colorants, hair tints, permanent waving
compositions, or hair gels.
46. The hair treatment composition as defined in claim 46 in
aerosol form, spray form or fluid form.
47. A process for treating hair comprising contacting hair with the
hair-treatment composition of claim 46.
Description
BACKGROUND OF THE INVENTION
[0001] The invention relates to compositions comprising quaternary
ammonium compounds which have a low setting point, good solubility
or dispersibility in aqueous media and a low flash point and are
thus highly suitable for formulating quaternary ammonium
compounds.
[0002] Cosmetic compositions, such as, for example, hair-treatment
compositions, often comprise sparingly water-soluble quaternary
ammonium compounds which have a long-chain alkyl or alkenyl group.
Such compositions are usually formulated as aqueous dispersions,
emulsions, microemulsions, gels or else in aerosol form and are
used, for example, as shampoos, hair cures, hair rinses, etc.
[0003] For the manufacturer of such compositions, it is highly
advantageous to prepare the quaternary ammonium compounds as
compounded materials or formulations in the form of flakes, pellets
or pastes which, as well as having a high cationic active
ingredient content, have a low setting point and good solubility or
dispersibility in aqueous media.
[0004] In accordance with the prior art, the above requirements can
be achieved by adding short-chain alcohols, in particular
isopropanol, in amounts of from 15 to 20% by weight. Because of
their low boiling and flash points, however, the use of such
short-chain alcohols is problematical.
[0005] As described in WO 00/28950, the short-chain alcohols can be
replaced by linear fatty alcohols (e.g. cetyl alcohol, lauryl
alcohol, behenyl alcohol or stearyl alcohol). In order to lower the
setting point of the mixtures to temperatures below 100.degree. C.,
glycols, such as, for example, propylene glycol or 1,3-butanediol,
are additionally added. WO 00/28950 further emphasizes that the
fatty alcohols are advantageously homogeneous fatty alcohols which
contain less than about 10% by weight of another fatty alcohol.
SUMMARY OF THE INVENTION
[0006] Surprisingly, it has now been found that compositions
comprising quaternary ammonium compounds, branched long-chain
alcohols, preferably mixtures of branched and unbranched long-chain
alcohols, and low molecular weight polyhydric alcohols have a low
setting point, good solubility and dispersibility in aqueous media
and a low flash point. Such compositions are thus highly suitable
for formulating quaternary ammonium compounds.
[0007] The invention provides compositions comprising
[0008] a) at least one quaternary ammonium compound according to
formula (1) 1
[0009] where
[0010] R.sub.1 is an unbranched or branched alkyl or alkenyl group
having 12 to 36 carbon atoms, a group R.sub.5CONH(CH.sub.2).sub.n--
or a group R.sub.5COO(CH.sub.2).sub.n--, where R.sub.5 is an alkyl
or alkenyl group having 12 to 36 carbon atoms and n is a number
from 1 to 8, and
[0011] R.sub.2, R.sub.3 and R.sub.4, independently of one another,
may be identical or different and are a --CH.sub.3,
CH.sub.3CH.sub.2--, CH.sub.3CH.sub.2CH.sub.2--,
CH.sub.3CH.sub.2CH.sub.2CH.sub.2--, --CH.sub.2CH.sub.2OH or
CH.sub.2CH(OH)CH.sub.2OH group and
[0012] X.sup.- is an anion, and
[0013] b) at least one branched alcohol b1) having 8 to 36 carbon
atoms or a mixture of at least one branched alcohol b1) and at
least one unbranched alcohol b2) having 8 to 36 carbon atoms,
and
[0014] c) at least one polyhydric alcohol having 2 to 6 carbon
atoms.
[0015] The branched alcohols b1) and unbranched alcohols b2) can be
saturated or unsaturated.
[0016] Particularly advantageous performance properties are
exhibited by compositions which comprise, as alcohol component b),
a mixture of at least one branched alcohol b1) and at least one
unbranched alcohol b2).
[0017] The proportion of quaternary ammonium compounds a), based on
the finished compositions, is preferably 30 to 90% by weight,
particularly preferably 50 to 90% by weight, especially preferably
60 to 90% by weight, very particularly preferably 60 to 80% by
weight.
[0018] Surprisingly, it has been found that the compositions can
advantageously have high proportions by weight of quaternary
ammonium compounds a) coupled with simultaneously low melting and
setting points.
[0019] Quaternary ammonium compounds a) are preferably
(C.sub.12-C.sub.36)-alkyltrimethylammonium compounds, particularly
preferably (C.sub.14-C.sub.30)-alkyltrimethylammonium compounds,
especially preferably (C.sub.16-C.sub.24)-alkyltrimethylammonium
compounds.
[0020] Particular preference is given to alkyltrimethylammonium
compounds in which the alkyl radical is a behenyl, erucyl, cetyl or
stearyl radical. The anion X.sup.- in formula (1) may be any
desired charge-balancing anion; preferably chloride, iodide,
bromide, methosulfate, hydrogensulfate, lactate and/or citrate,
particularly preferably chloride and methosulfate.
[0021] A very particularly suitable quaternary ammonium compound a)
is behenyltrimethylammonium chloride.
[0022] The proportion of alcohol component b) is, based on the
finished compositions, preferably 10 to 60% by weight, particularly
preferably 10 to 50% by weight, especially preferably 20 to 40% by
weight.
[0023] If the compositions comprise branched alcohols b1) and
unbranched alcohols b2), then the weight ratio of branched alcohols
b1) to unbranched alcohols b2) is preferably 90:10 to 10:90,
particularly preferably 70:30 to 30:70, especially preferably 60:40
to 40:60.
[0024] Preferably, the branched alcohols b1) and the unbranched
alcohols b2) have 10 to 24, particularly preferably 12 to 18,
especially preferably 14 to 16, carbon atoms. The branched alcohols
b1) are preferably singly branched.
[0025] Particularly suitable branched alcohols b1) are Guerbet
alcohols, 2-methyl-1-decanol, 2-ethyl-1-nonanol,
2-propyl-1-octanol, 2-butyloctanol, 2-butyldecanol, 2-hexyloctanol,
2-hexyldecanol, 2-octyldecanol, 2-hexyldodecanol, 2-octyldodecanol,
2-decyltetradecanol, 2-butyl-1-heptanol, 2-dodecylhexadecanol,
tetradecyloctadecanol, 2-tetradecyleicosanol,
2-hexadecyloctadecanol, 2-hexadecyleicosanol, 2-methyltridecanol,
2-ethyldodecanol, 2-propylundecanol, 2-pentylnonanol,
2-heptylheptanol, 2-methyltetradecanol, 2-ethyltridecanol,
2-propyldodecanol, 2-butylundecanol, 2-pentyldecanol,
2-hexylnonanol, 2-heptyloctanol, isotridecyl alcohol and mixtures
thereof.
[0026] Particular preference is given to compositions which
comprise, as branched alcohols b1), alcohol mixtures corresponding
to the commercially available .RTM.Isalchem grades (Sasol).
[0027] Preferred branched alcohols b1) for the combined use with
unbranched alcohols b2) are 2-methyltridecanol, 2-ethyldodecanol,
2-propylundecanol, 2-butyidecanol, 2-pentylnonanol, 2-hexyloctanol,
2-heptylheptanol, 2-methyltetradecanol, 2-ethyltridecanol,
2-propyidodecanol, 2-butylundecanol, 2-pentyldecanol,
2-hexylnonanol and 2-heptyloctanol.
[0028] Preferred unbranched alcohols b2) are fatty alcohols,
particularly preferably lauryl alcohol, myristyl alcohol, cetyl
alcohol, stearyl alcohol, eicosanyl alcohol and behenyl alcohol.
Likewise preferred are nonanol, undecanol, tridecanol, pentadecanol
and heptadecanol.
[0029] In a particularly preferred embodiment, the compositions
comprise branched alcohols b1) and unbranched alcohols b2) having
in each case 14 to 16 carbon atoms, where the weight ratio, based
on the finished compositions, of branched alcohols b1) to
unbranched alcohols b2) is 70:30 to 30:70, particularly preferably
65:35 to 55:45, especially preferably 60:40, and the weight ratio
of alcohols having 14 carbon atoms to alcohols having 15 carbon
atoms is in the range from 55:45 to 65:35.
[0030] Particular preference is given to compositions which
comprise, as mixtures of branched alcohols b1) and unbranched
alcohols b2), alcohol mixtures corresponding to the .RTM.LIAL
grades (e.g. .RTM.LIAL 145 and 123, Sasol). The alcohols from the
.RTM.LIAL grades are typically prepared by the oxo process.
[0031] The proportion of polyhydric alcohols c) is, based on the
finished compositions, preferably 0.5 to 20% by weight,
particularly preferably 0.5 to 10% by weight.
[0032] Polyhydric alcohols c) are to be understood as meaning
alcohols with at least two OH groups.
[0033] Preference is given to glycols, particular preference is
given to ethylene glycol and propylene glycol, butanediols,
particularly preferably 1,3-butanediol, glycerol, thioglycerol,
sorbitol, xylitol and mannitol.
[0034] Particular preference is given to propylene glycol, glycerol
and 1,3-butanediol.
[0035] Optionally, to improve the performance properties, the
compositions according to the invention may comprise unbranched or
branched monoalcohols having 1 to 4 carbon atoms. Preferred
monoalcohols are ethanol, propanol, isopropanol, butanol,
isobutanol and tert-butanol, particularly preferably isopropanol.
Based on the finished compositions, the compositions preferably
comprise less than 5% by weight, particularly preferably less than
1% by weight, of such monoalcohols. In a likewise preferred
embodiment, the compositions are free from such monoalcohols.
[0036] The compositions according to the invention preferably have
a setting point below 100.degree. C., particularly preferably below
95.degree. C., especially preferably below 90.degree. C., very
particularly preferably 85.degree. C.
[0037] The flash point of the compositions according to the
invention is preferably above 80.degree. C., particularly
preferably above 100.degree. C.
[0038] The compositions according to the invention may, for
example, be pellets, flakes, extrudates, pastes, compacts, powders,
and also emulsions or dispersions.
[0039] In a preferred embodiment, the compositions according to the
invention are prepared by preparing a mixture comprising
[0040] i) at least one quaternary ammoniun compound a), optionally
containing a branched or unbranched monoalcohol having 1 to 4
carbon atoms,
[0041] ii) at least one branched alcohol b1) having 8 to 36 carbon
atoms or a mixture of at least one branched alcohol b1) and at
least one unbranched alcohol b2) having 8 to 36 carbon atoms,
[0042] iii) at least one polyhydric alcohol c) and
[0043] iv) optionally at least one unbranched or branched
monoalcohol having 1 to 4 carbon atoms.
[0044] In a preferred embodiment, the components i) to iv) are
mixed and then heated, optionally with stirring. Here, the
temperature is chosen so that the mixture is in the form of a melt.
Preference is given to temperatures of from 70 to 120.degree. C.,
particularly preferably 80 to 110.degree. C. In another preferred
embodiment, the component i) is introduced as a melt.
[0045] The quaternary ammonium compounds a) of component i) can be
prepared in a known manner by alkylation of a tertiary amine in the
presence of at least one unbranched or branched monoalcohol having
1 to 4 carbon atoms, preferably ethanol, propanol, isopropanol,
butanol, isobutanol and tert-butanol, particularly preferably
isopropanol. The quaternary ammonium compounds are preferably used
as pellets or particularly preferably as powders. In a preferred
embodiment, the quaternary ammonium compounds comprise less than 5%
by weight, preferably less than 2% by weight, of monoalcohols. In a
further preferred embodiment, the quaternary ammonium compounds
comprise 10 to 25% by weight of monoalcohols. The compositions
according to the invention preferably have a total content of
unbranched or branched monoalcohols having 1 to 4 carbon atoms of
less than 5% by weight, particularly preferably less than 1% by
weight.
[0046] In a likewise preferred embodiment, the compositions
according to the invention are free from unbranched or branched
monoalcohols having 1 to 4 carbon atoms.
[0047] To establish the desired content of monoalcohols in the
compositions according to the invention, the components i) and/or
iv) are correspondingly chosen and calculated and/or the
monoalcohols are partially or completely removed from the component
i) beforehand.
[0048] In a further embodiment, the monoalcohols are subsequently
removed from the compositions according to the invention except for
the desired residual content. The monoalcohols are preferably
stripped off at 700 to 10 mbar, preferably 400 to 70 mbar, and 60
to 90.degree. C.
[0049] The monoalcohols can also be distilled off at atmospheric
pressure in suitable evaporation devices (e.g. thin-film
evaporator) at temperatures up to 120.degree. C.
[0050] Surprisingly, it has been found that the compositions
according to the invention can also be prepared "in situ" by
alkylation of
[0051] i) at least one tertiary amine NR.sub.1R.sub.2R.sub.3,
[0052] where
[0053] R.sub.1 is an unbranched or branched alkyl or alkenyl group
having 12 to 36 carbon atoms, a group R.sub.5CONH(CH.sub.2).sub.n--
or a group R.sub.5COO(CH.sub.2).sub.n--, where R.sub.5 is an alkyl
or alkenyl group having 12 to 36 carbon atoms and n is a number
from 1 to 8, and R.sub.2 and R.sub.3, independently of one another,
may be identical or different and are --CH.sub.3--,
CH.sub.3CH.sub.2--, CH.sub.3CH.sub.2CH.sub.2--,
CH.sub.3CH.sub.2CH.sub.2CH.sub.2-- or --CH.sub.2CH.sub.2(OH),
by
[0054] ii) at least one alkylating agent chosen from
[0055] a) R.sub.4X, where R.sub.4 is --CH.sub.3,
CH.sub.3CH.sub.2--, CH.sub.3CH.sub.2CH.sub.2--,
CH.sub.3CH.sub.2CH.sub.2CH.sub.2-- or --CH.sub.2CH(OH)CH.sub.2(OH),
and X is Cl, I, Br, OSO.sub.3H or methosulfate, and/or
[0056] b) ethylene oxide and an acid HX, where X is Cl, I, Br,
OSO.sub.3H, citrate or lactate,
[0057] in the presence of
[0058] iii) at least one branched alcohol b1) having 8 to 36 carbon
atoms or a mixture of at least one branched alcohol b1) and one
unbranched alcohol b2) having 8 to 36 carbon atoms and
[0059] iv) at least one polyhydric alcohol c) and
[0060] v) optionally at least one unbranched or branched
monoalcohol having 1 to 4 carbon atoms.
[0061] Preferably, in the reaction, the feed amounts of branched
alcohols b1), unbranched alcohols b2), polyhydric alcohols c) and
optionally unbranched or branched monoalcohol having 1 to 4 carbon
atoms are chosen to correspond to the composition already described
above as preferred for the compositions according to the invention.
The contents can also be adjusted by subsequent addition or
removal.
[0062] In a preferred embodiment, no unbranched or branched
monoalcohols having 1 to 4 carbon atoms are used in the
reaction.
[0063] The compositions according to the invention prepared by the
above-described processes can be converted as homogeneous or
inhomogeneous melts by cooling into pellets, flakes, extrudates or
pastes or, after cooling, be further processed to give compacts,
powders, granulates, emulsions or dispersions.
[0064] The compositions according to the invention are generally
suitable for the preparation of compositions comprising quaternary
ammonium compounds. The compositions are particularly suitable for
the preparation of cosmetic, dermatological and pharmaceutical
compositions. In particular, they are suitable for the preparation
of hair-treatment compositions.
[0065] The invention accordingly also provides for the use of the
compositions according to the invention for the preparation of
compositions, preferably cosmetic, dermatological and
pharmaceutical compositions, in particular hair-treatment
compositions, comprising quaternary ammonium compounds. Examples of
preferred compositions are shampoos, rinse-off hair conditioners,
cream rinses, clear rinses, hair cures, hair colorants and hair
tints, permanent waving compositions, hair gels, hair conditioners
in aerosol, spray and fluid form, 2-in-1 shower preparations, cream
shower preparations, skincare compositions, day creams, night
creams, care creams, nutrient creams, body lotions and
ointments.
[0066] The cosmetic, dermatological and pharmaceutical compositions
comprise the compositions according to the invention, based on the
finished compositions, preferably in amounts of from 0.1 to 15% by
weight, particularly preferably 1 to 10% by weight, particularly
preferably 1 to 7% by weight.
[0067] The cosmetic, dermatological and pharmaceutical compositions
can comprise, as further auxiliaries and additives, all customary
surfactants, oily substances, emulsifiers and coemulsifiers,
cationic polymers, film formers, super fatting agents,
moisture-donating agents, stabilizers, biogenic active ingredients,
glycerol, preservatives, pearlizing agents, dyes and fragrances,
solvents, hydrotropic agents, opacifiers, thickeners, dispersants,
protein derivatives, such as gelatins, collagen hydrolyzates,
natural and synthetic-based polypeptides, egg yolk, lecithin,
lanolin and lanolin derivatives, fatty alcohols, silicones,
deodorizing agents, substances with a keratolytic and keratoplastic
action, enzymes, carrier substances, antioxidants, UV light
protection filters, pigments and metal oxides, and antimicrobially
effective agents.
[0068] The surfactants used may be anionic, cationic, nonionic,
amphoteric and/or zwitterionic surfactants. Preferred nonionic
surfactants contain, as hydrophilic group, a polyol group, a
polyolalkenyl ether group, or a combination of polyol and
polyglycol ether groups. Preference is given to addition products
of from 2 to 30 mol of ethylene oxide, 2 to 30 mol of ethylene
oxide together with up to 5 mol of propylene oxide or of up to 5
mol of propylene oxide onto linear fatty alcohols having 8 to 22
carbon atoms and alkylphenols having 8 to 15 carbon atoms in the
alkyl group, (C.sub.12-C.sub.19)-fatty acid mono- and diesters of
addition products of from 1 to 30 mol of ethylene oxide onto
glycerol, glycerol mono- and diesters and sorbitan mono- and
diesters of saturated and unsaturated (C.sub.8-C.sub.18)-fatty
acids and ethylene oxide addition products thereof,
(C.sub.8-C.sub.18)-alkylmono- and oligoglycosides and ethoxylated
analogs thereof, addition products of from 10 to 60 mol of ethylene
oxide onto castor oil and hydrogenated castor oil, ethoxylated and
nonethoxylated mono-, di- and trialkyl monophosphoric esters, in
particular mono-, di- and tri(lauryl tetraglycol ether)
o-phosphoric esters and mono-, di- and tri(cetyl tetraglycol ether)
o-phosphoric esters.
[0069] Preferred amphoteric surfactants carry a
(C.sub.8-C.sub.18)-alkyl or acyl group and at least one free amino
group and at least one --COOH or --SO.sub.3H group. Preference is
given to N-acylglycines, N-alkylpropionic acid, N-alkylaminobutyric
acids, N-alkyliminodipropionic acids,
N-hydroxyethyl-N-alkylamidopropylglycines, N-alkyltaurines,
N-alkylsarcosines, 2-alkylaminopropionic acids and alkylaminoacetic
acids having in each case 8 to 18 carbon atoms in the alkyl group.
Particular preference is given to N-cocoalkylaminopropionate,
cocoacylaminoethylaminopropionate and
(C.sub.12-C.sub.18)-alkylsarcosines- .
[0070] Particularly suitable zwitterionic surfactants are betaines,
such as, for example, N-alkyl-N,N-dimethylammonium glycinates, e.g.
cocoalkyldimethylammonium glycinates,
N-acylaminopropyl-N-N-dimethylammon- ium glycinates, e.g.
cocoacylaminopropyldimethylammonium glycinate,
2-alkyl-3-carboxymethyl-3-hydroxyethylimidazolines having in each
case 8 to 18 carbon atoms in the alkyl or acyl group and
cocoacylaminoethyl hydroxyethylcarboxymethyl glycinate.
[0071] The compositions preferably comprise surfactant mixtures,
particular preference being given to mixtures of nonionic and
zwitterionic or amphoteric surfactants in a weight ratio of from
5:1 to 1:5 or mixtures of nonionogenic surfactants and any desired
mixtures of zwitterionic and amphoteric surfactants in a weight
ratio of from 5:1 to 1:5.
[0072] Suitable oily substances are all known oils, fats and waxes
of mineral, animal, vegetable and synthetic origin. Preference is
given, as oil and fatty components, to diallyl ethers having a
total of 12 to 24 carbon atoms, fatty acid esters having a total of
12 to 26 carbon atoms, liquid hydrocarbons having 10 to 32 carbon
atoms and mixtures thereof. Suitable fatty acid esters are, for
example, methyl palmitate, ethyl oleate, isopropyl myristate,
n-hexyl laurate, n-butyl stearate and cetyl/stearyl
isononanoate.
[0073] Particular preference is given to paraffin oils, vaseline,
vegetable oils, synthetic triglycerides, such as, for example,
glyceryl tricaprylate, and also silicone oils.
[0074] Super fatting agents which may be used are substances such
as, for example, lanolin and lecithin, and polyethoxylated or
acylated lanolin and lecithin derivatives, polyol fatty acid
esters, monoglycerides and fatty acid alkanolamides.
[0075] Suitable bodying agents are fatty alcohols having 12 to 22,
preferably 12 to 18, carbon atoms, and also partial glycerides.
[0076] Further thickeners which may be used are polysaccharides, in
particular xantham gum, guar-guar, agar-agar, alginates,
carboxymethylcellulose, hydroxyethylcellulose, relatively high
molecular weight polyethylene glycol mono- and diesters of fatty
acids, polyacrylates, polyvinyl alcohol and polyvinylpyrrolidone,
surfactants such as, for example, ethoxylated fatty acid
glycerides, esters of fatty acids with polyols such as, for
example, pentaerythritol or trimethylpropane, fatty alcohol
ethoxylates or alkyl oligoglucosides, and electrolytes, such as
sodium chloride and ammonium chloride.
[0077] Examples of suitable silicone compounds are
dimethylpolysiloxane, methylphenylpolysiloxanes, cyclic silicones,
and amino-, fatty acid-, alcohol-, polyether-, epoxy-, fluorine-
and/or alkyl-modified silicone compounds which, at room
temperature, may either be in liquid form or in the form of a
resin.
[0078] Biogenic active ingredients are to be understood as meaning,
for example, Bisabolol.RTM., Allantoin.RTM., Phytantriol.RTM.,
Panthenol.RTM., AHAs, plant extracts and vitamin complexes.
[0079] Antidandruff agents which can be used are Climbazole.RTM.,
Octopirox.RTM., Oxiconazole.RTM. and Zinc Pyrethione.RTM..
[0080] Customary film formers are chitosan, microcrystalline
chitosan, quaternized chitosan, polyvinylpyrrolidone,
vinylpyrrolidone-vinyl acetate copolymers, polymers of the acrylic
acid series, quaternary cellulose derivatives, collagen, hyaluronic
acid and salts thereof and similar compounds.
[0081] To improve the flow behavior, hydrotropic agents, such as,
for example, ethanol, isopropyl alcohol, propylene glycol or
glucose, can also be used.
[0082] Suitable preservatives are, for example, phenoxyethanol,
formaldehyde solution, parabens, pentanediol and sorbic acid.
[0083] An available moisture-donating substance is, for example,
isopropyl palmitate, glycerol and/or sorbitol.
[0084] The total content of auxiliaries and additives in the
compositions is preferably 1 to 50% by weight, particularly
preferably 5 to 40% by weight.
[0085] The examples below serve to illustrate the invention, but do
not limit it.
EXAMPLES
[0086] a) Quaternary Ammonium Compounds (Behenyltrimethylammonium
Chloride)
[0087] Behenyltrimethylammonium chloride prepared in the solvent
isopropanol was dried in the form of pellets to remove the solvent
in a vacuum oven for 14 hours at a temperature of 74.degree. C. and
a pressure of 200 mbar until the weight was constant. The pellets
dried in this way were ground to give a powder and sieved (sieve
width: 630 .mu.m).
[0088] b) Preparation of the Compositions According to the
Invention:
[0089] The behenyltrimethylammonium chloride powder obtained in a)
was mixed with a branched alcohol b1) or a mixture of branched
alcohols b1) and unbranched alcohols b2) and a polyhydric alcohol
c). The mixtures were then homogenized in a sealed powder bottle in
a drying cabinet with heating and repeated stirring until the
powder had completely dissolved. By slowly reducing the temperature
in the drying cabinet, the setting points were determined. The quat
activity was determined by cation titration.
Example 1
[0090] 6.7 g of dried and sieved behenyltrimethylammonium chloride
was introduced into a 50 ml powder bottle made of glass and treated
with 3.0 g of .RTM.LIAL 145 (Sasol) and 0.3 g of an 87% strength by
weight aqueous glycerol solution. After the bottle had been sealed,
the mixture was heated at about 100.degree. C. for 12 hours. During
this period, the sample was stirred a number of times using a
spatula in order to homogenize the mixture. This gave a clear,
slightly yellowish solution which solidified at 80-84.degree. C.
and was completely molten again at 90.degree. C. At 25.degree. C.,
the composition was wax-like solid. The quat active content was 67%
by weight.
Example 2
[0091] 6.5 g of dried and sieved behenyltrimethylammonium chloride
was introduced into a 50 ml powder bottle made of glass and treated
with 2.9 g of .RTM.LIAL 145 (Sasol) and 0.6 g of propylene glycol.
After the bottle had been sealed, the mixture was heated at about
100.degree. C. for 4 hours and at 90.degree. C. for a further 12
hours. During this period, the sample was stirred a number of times
using a spatula in order to homogenize the mixture. This gave a
clear, slightly yellowish solution which slowly solidified at
76-81.degree. C. and was completely clear and molten again at
90.degree. C. At 25.degree. C., the composition was wax-like solid.
The quat active content was 65% by weight.
Example 3
[0092] 7.0 g of dried and sieved behenyltrimethylammonium chloride
was introduced into a 50 ml powder bottle made of glass and treated
with 2.4 g of .RTM.LIAL 145 (Sasol) and 0.6 g of propylene glycol.
After the bottle had been sealed, the mixture was heated at about
100.degree. C. for 4 hours and at 90.degree. C. for a further 12
hours. During this period, the sample was stirred a number of times
using a spatula in order to homogenize the mixture. This gave a
clear, slightly yellowish solution which slowly solidified at
80-84.degree. C. and was completely clear and molten again at
90.degree. C. At 25.degree. C., the composition was wax-like solid.
The quat active content was 70% by weight.
Example 4
[0093] 6.7 g of dried and sieved behenyltrimethylammonium chloride
was introduced into a 50 ml powder bottle made of glass and treated
with 2.8 g of .RTM.LIAL 145 (Sasol) and 0.5 g of 1,3-butanediol.
After the bottle had been sealed, the mixture was heated at about
100.degree. C. for 16 hours. During this period, the sample was
stirred a number of times using a spatula in order to homogenize
the mixture. This gave a clear, slightly yellowish solution which
slowly solidified at 95-97.degree. C. and was completely clear and
molten again at 100.degree. C. At 25.degree. C., the composition
was wax-like solid. The quat active content was 67% by weight.
Example 5
[0094] 4.88 g of dried and sieved behenyltrimethylammonium chloride
was introduced into a 50 ml powder bottle made of glass and treated
with 4.61 g of .RTM.LIAL 145 (Sasol) and 0.51 g of 1,3-butanediol.
After the bottle had been sealed, the mixture was heated at about
100.degree. C. for 4 hours and at 90.degree. C. for a further 12
hours. During this period, the sample was stirred a number of times
using a spatula in order to homogenize the mixture. This gave a
clear, slightly yellowish solution which slowly solidified at
68-72.degree. C. and was completely clear and molten again at
90.degree. C. At 25.degree. C., the composition was wax-like solid.
The quat active content was 48% by weight.
Comparative Example 4a
[0095] 4.88 g of dried and sieved behenyltrimethylammonium chloride
was introduced into a 50 ml powder bottle made of glass and treated
with 4.61 g of cetyl alcohol and 0.51 g of 1,3-butanediol. After
the bottle had been sealed, the mixture was heated at about
100.degree. C. for 4 hours and 90.degree. C. for a further 12
hours. During this period, the sample was stirred a number of times
with a spatula in order to homogenize the mixture. This gave a
clear solution which slowly solidified at 84-86.degree. C. and was
completely clear and molten again at 90.degree. C.
[0096] Examples 6 to 8 give formulation examples. The compositions
according to the invention were pelletized by being dropped onto a
cold metal plate and then incorporated into the formulations.
Example 6
Cream Rinse
[0097]
1 A Composition according to the invention Ex. 12.2% by weight
.RTM.HOSTAPHAT KL 340 D 1.5% by weight (trilaureth-4 phosphate,
Clariant) Cetyl alcohol 3% by weight Paraffin oil 1% by weight B
Water 92.3% by weight C Citric acid q.s.
[0098] Preparation:
[0099] I) Melt A at 75.degree. C.
[0100] II) Heat B to 75.degree. C.
[0101] III) Stir B into A and further stir the mixture until
cool
[0102] IV) Adjust pH to pH=4 using C.
Example 7
O/W Handcream
[0103]
2 A Composition from Ex. 1 3% by weight .RTM.Hostacerin DGSB 6% by
weight (PEG-4 polyglycerol-2-stearate, Clariant) Paraffin oil, high
viscosity 10% by weight Isopropyl palmitate 10% by weight B Water
70.6% by weight Preservative q.s. C Perfume 0.4% by weight
[0104] Preparation:
[0105] I) Melt A at 80.degree. C.
[0106] II) Heat B to 80.degree. C.
[0107] III) Stir B into A and further stir the mixture until
cool
[0108] IV) Add C to III at 35.degree. C.
Example 8
Hair Conditioner with Pearlescent Effect
[0109]
3 A Composition from Ex. 1 2.2% by weight .RTM.Genamin KSL 9% by
weight (PEG-5 stearyl ammonium lactate, Clariant) .RTM.Hostaphat KL
340 D 1.5% by weight (trilaureth-4 phosphate, Clariant) Jojoba oil
1% by weight B .RTM.Tylose H 100 000 YP2 1.5% by weight
(Hydroxyethylcellulose, Clariant) C Water ad 100% D Perfume 0.5% by
weight Panthenol 0.5% by weight Genapol PDC (Clariant) 4% by weight
(Glycol distearate, laureth-4, cocamidopropyl betaine, mica,
titanium dioxide) E Citric acid q.s.
[0110] Preparation:
[0111] I) Heat components A to 75.degree. C.
[0112] II) Dissolve B well in C and heat to 75.degree. C.
[0113] III) Add II to I with stirring
[0114] IV) Allow to cool with stirring and add the components D to
III at 30.degree. C. one after the other
[0115] V) Adjust pH to pH=4 using E.
* * * * *